molecular biology scientist

Cellular Intelligence

<div>About Cellular Intelligence 
Cellular Intelligence (CI) is an AI-native TechBio company building a universal foundation model of cell signaling to understand, predict, and ultimately control cellular behavior, transforming biology from trial-and-error into an engineering discipline. We take a full-stack approach, generating perturbation data at over 1,000x the efficiency of conventional methods, capturing millions of time-resolved treatment combinations per experiment, and training large-scale models that generalize across contexts to enable rational protocol design for regenerative medicine, context-specific drug effect prediction, and systematic disease modeling. Our founding team includes repeat AI entrepreneur Dr. Micha Breakstone (Chorus.ai, acquired for $575M), the Head of the Fundamental AI Group at MIT, and four professors from Harvard Medical School and the University of Washington, including the Chair of Genetics at Harvard, collectively holding five National Academy memberships. Based in Boston, CI has raised over $60M to date from Khosla Ventures, CZI, SciFi VC, and AMD Ventures, and is rapidly scaling its world-class team. 
 
Cellular Intelligence&rsquo;s Core Values<ul><li>
We show up - fully accountable, all-in, doing whatever it takes.</li><li>
We act with urgency - swift, decisive, proactive.</li><li>
We support one another - collaborative, helpful, empathetic.</li></ul> 
Location: Boston, MA
Reports to: Senior Principal Scientist, Molecular Biology
About the role<ul><li>
Execute Next Generation Sequencing (NGS) workflows for DNA and RNA sequencing library preparation.</li><li>
Support technology development, troubleshooting, and scale-up for high-throughput workflows.</li><li>
Maintain clear, organized records of experimental design and execution in electronic laboratory notebooks (ELN) such as Benchling.</li><li>
Collaborate with wet lab and computational teams to support and provide updates on research progress.</li></ul>
About you<ul><li>
BA/BS and MS in Molecular Biology, Biochemistry, Genomics, or a related field.</li><li>
1-2 years of hands-on experience in generating NGS libraries in an industry setting.</li><li>
Proficiency in molecular biology techniques, including PCR and qPCR.</li><li>
Detail-oriented with strong documentation and organizational skills.</li><li>
Familiarity with Illumina sequencing library preparation and sample QC such as concentration and size evaluation.</li><li>
Excellent communication skills, both written and verbal.</li><li>
Experience with inventory tracking and reagent QC.</li><li>
Experience in single cell sequencing, long-read sequencing, or other sequencing platforms a plus.</li><li>
Experience with assay development, automation, or high-throughput sample processing.</li><li>
Comfortable operating in fast-paced, startup or early-phase biotech environments.</li></ul>
Benefits:<ul><li>
Take a technical leadership role with a mission-driven company with the potential to significantly impact the lives of millions</li><li>
Work alongside a talented and passionate team at the forefront of AI and cellular biology</li><li>
Contribute to the development of groundbreaking therapies that address significant unmet medical needs</li><li>
Enjoy a competitive salary and benefits package, including flexible work options</li></ul>
Exceptional candidates who demonstrate outstanding capabilities and potential will be considered, even if they do not meet every qualification listed.
Join us and help unlock the full potential of AI for the benefit of human health!
Cellular Intelligence is committed to equal employment opportunity and non-discrimination for all employees and applicants regardless of race, color, ancestry, sex, sexual orientation, age, religion, national origin, ancestry, genetic information, disability, veteran status, marital status, citizenship status, or any characteristic protected under applicable law.</div>

Research Associate, Molecular Biology

New York Genome Center

<div>We are looking for a highly motivated, independent and team-oriented Associate Scientist I to work in our high throughput production lab&rsquo;s Quality Control (QC) Team responsible for initial sample handling. Main responsibilities include, nucleic acid extractions, initial sample QC, and genotyping on the Illumina Infinium platform. This position reports to the QC Supervisor.

Key Responsibilities
<ul>
<li>Carry out procedures associated with DNA &amp; RNA for sequencing platforms, including DNA/RNA sample extraction, quantification &amp; preparation, Illumina Infinium genotyping,
</li>
<li>Assist with library preparation and sequencer operation for Illumina NovaSeq X, Ultima UG100, Oxford Nanopore PromethION, PacBio Revio platforms, as needed;
</li>
<li>Perform quality control of initial samples and sequencing ready final library samples;
</li>
<li>Perform sample nucleic acid extraction with the use of automation (Hamilton Star, KingFisher Flex, QIAcube Connect);
</li>
<li>Process DNA for Illumina microarray platforms with use of automation (Hamilton Star, Tecan, iScan);
</li>
<li>Conduct other laboratory work, as needed;
</li>
<li>Track all work and issues in the appropriate databases and Laboratory Information Management Systems (LIMS);
</li>
<li>Become proficient using NYGC&rsquo;s LIMS tracking system to accurately perform day-to-day tasks;
</li>
<li>Perform monthly instrument maintenance on laboratory equipment, in accordance to instrument SOPs Equipment maintenance
</li>
</ul>Requirements &amp; Qualifications
<ul>
<li>Bachelors&rsquo; degree in Molecular Biology, Biotechnology, Biochemistry or related field, plus laboratory experience in nucleic acid research required;
</li>
<li>1 year of experience in a molecular biology lab;
</li>
<li>Experience with automated liquid handlers preferred;
</li>
<li>Experience in next-generation sequencing a plus;
</li>
<li>Solid knowledge of molecular biology equipment and related protocols (including RNA and DNA preparation, RNA and DNA quantification, hybridization, PCR, multiplex amplification and bead-based solutions) highly preferred;
</li>
<li>Familiarity with Microsoft Word, Excel, and PowerPoint, preferably with Mac OS;
</li>
<li>Good general laboratory and organizational skills, including the ability to work independently and efficiently are essential;
</li>
<li>Ability to multitask is a must, along with an orientation toward teamwork and cooperation;
</li>
<li>Strong creative thinking and problem-solving skills; and,
</li>
<li>Excellent communication skills required.
</li>
</ul>Competencies
<ul>
<li>Technical and Professional Skills: Consistently demonstrates skills and knowledge relevant for current role; strives to expand the depth and breadth of technical and professional skills; works with a high level of integrity; exhibits focus and discipline; appropriately prioritizes, manages expectations and delivers on commitments.
</li>
<li>Collaborative &amp; Communicative: Models collaboration and teamwork; brings out the best in others; effectively works with all levels, internally and externally; respects and embraces diversity of perspective; communicates clearly and listens carefully; uses good judgment as to what to communicate and when to do so.
</li>
<li>Adaptable &amp; Innovative: Adaptable and embraces change; develops new insights and pursues improvements and efficiency; fosters exchange of new ideas and willing to challenge the status quo; takes initiative and is solution-oriented; engages in work with passion and curiosity.
</li>
</ul>Salary &amp; Benefits

The pay range for this position is $57,000-67,000 per year; the base pay offered may vary depending on job-related knowledge, skills, and experience.

In addition, NYGC offers a full range of medical, financial, and other benefits as well as generous time off. This includes Medical/Dental/Vision for employees &amp; dependent(s); Vacation, Holidays, Sick, and Other Leave, including a paid winter break; a 401(k) match; Life Insurance; Flexible Spending Accounts; employee Tuition Reimbursement; flexible schedules and telework options for some positions; an Employee Assistance Program; and much more.

About the New York Genome Center

The New York Genome Center (NYGC) is an independent, nonprofit, academic research organization dedicated to advancing genomic research. NYGC scientists and staff are furthering new approaches to diagnosing and treating neurological diseases and cancer through their unique capabilities in whole genome sequencing, RNA sequencing, state-of-the art analytics, and the development of genomic tools. NYGC concentrates specifically on disease-based research in the following areas: neuropsychiatric disease (autism, schizophrenia, bipolar); neurodegenerative disease (ALS, Alzheimer&rsquo;s, Parkinson&rsquo;s, Huntington&rsquo;s), and cancer.

Located in Lower Manhattan, the New York Genome Center was founded by and remains closely affiliated with twelve leading academic medical centers and research universities in the New York region and beyond, engaging in research projects with and for these institutions. Essential to our collaborative work is an outstanding faculty, whose members typically hold a joint appointment at NYGC and a partner university. They support our scientific mission by conducting independent research in areas of mutual interest to us and the wider scientific community.

Equal Opportunity

We are committed to fostering a workplace environment that is welcoming and fair to all, ensuring that every employee has the opportunity to thrive. We believe that bringing together individuals with diverse backgrounds, experiences, and perspectives leads to greater collaboration, innovation, and discovery. Valuing and supporting each employee in reaching their full potential strengthens our organization and enhances our collective success. We recognize that creating an environment where all employees feel valued and included requires sustained effort and dedication from the entire organization.

The New York Genome Center is a VEVRAA Federal Contractor. All qualified applicants will receive consideration for employment and will not be discriminated against on the basis of race, creed, color, gender, religion, national origin, sexual orientation, age, disability, genetic predisposition or carrier status, protected veteran or military status, domestic violence victim status, partnership status, caregiver status, alienage or citizenship status, marital status, or any other characteristic protected by applicable law. NYGC takes affirmative action in support of its policy to hire and advance in employment individuals who are protected veterans and individuals with disabilities.

FLSA Status &ndash; Exempt

This position is not eligible for visa sponsorship or relocation assistance.</div>

Associate Scientist I, Production Lab

Natera

<div>POSITION SUMMARY:

The Associate Scientist within the Molecular Biology product development team will join a cross-functional team of scientists who are tasked with developing and advancing Natera's oncology product portfolio.

The Associate scientist will be working with internal cross functional teams and investigating the feasibility of applying a variety of scientific principles and concepts to oncology diagnostics and monitoring space. The ideal candidate is a driven professional who maintains broad knowledge of state-of-the-art principles and theories with an in-depth understanding of applicability to oncology research. This position requires flexibility to work outside standard business hours, including some evenings and weekends, to address urgent issues, support high-priority projects, and maintain uninterrupted lab operations.

We are looking for a meticulous and dedicated scientist with experience in both assay development and high throughput automation that can work effectively in a fast-paced environment to ensure that the highest quality clinical assays are developed and launched for our patients.

PRIMARY RESPONSIBILITIES:
<ul>
<li>Design, develop, and validate automated high-throughput NGS assays that will be run in a commercial CLIA laboratory</li>
<li>Participate in post-launch surveillance by troubleshooting production issues, performing root cause analysis on automation, reagent, peripheral equipment and assay failures</li>
<li>Independently design and execute moderate to high complexity experiments</li>
<li>Collaborate with assay development scientists on the specifications of assay, reagent, equipment and quality metrics for existing and future production assays</li>
<li>Work with Clinical Laboratory and Quality Assurance to ensure that developed methods meet Natera's rigorous quality standards</li>
<li>Coordinate across multiple internal groups (automation engineering, laboratory operations, bioinformatics, statistics, project and product management) and serve as point person to ensure the successful identification and timely execution of projects</li>
<li>Write documentation and SOPs, and train lab operations operators on protocols</li>
<li>Oversee validation activities</li>
<li>Identify areas for continuous improvement and actively contribute to the effort of introducing better practices to improve production workflows and shorten TAT for patient samples</li>
</ul>
QUALIFICATIONS:
<ul>
<li>BA/BS with 6 years experience or MS with 3 years experience in assay development and automation for the genomics</li>
<li>Demonstrated track record of development and validation of automated protocols for CLIA</li>
</ul>
KNOWLEDGE, SKILLS, AND ABILITIES:
<ul>
<li>Strong understanding of the chemistry underlying nucleic acid extraction, PCR, NGS library preparation, and hybrid capture technologies</li>
<li>Hands-on experience in reagent preparation and quality control for NGS-based assays</li>
<li>Experience implementing, optimizing, and troubleshooting high-throughput automated assays utilizing liquid handler robots</li>
<li>Data analysis (JMP) required, coding skills (Python or R) are a plus</li>
<li>Strong individual contributor as well as dedicated team player</li>
<li>Experience designing and executing studies including stability, guard banding, reproducibility and repeatability, and validation</li>
<li>Experience working in a regulated laboratory environment under CLIA/CAP, NYSDOH, IVD is a plus</li>
<li>Excellent communication, organizational, record-keeping, planning, attention to detail and time management skills</li>
<li>Ability to collaborate cross-functionally with other groups (CLIA, lab operations QA, Automation, Research)</li></ul><div> 
OUR OPPORTUNITY

Natera&trade; is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women's health, and organ health. Our aim is to make personalized genetic testing and diagnostics part of the standard of care to protect health and enable earlier and more targeted interventions that lead to longer, healthier lives.

The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory scientists, business professionals, software engineers and many other professionals from world-class institutions, who care deeply for our work and each other. When you join Natera, you'll work hard and grow quickly. Working alongside the elite of the industry, you'll be stretched and challenged, and take pride in being part of a company that is changing the landscape of genetic disease management.

WHAT WE OFFER

Competitive Benefits - Employee benefits include comprehensive medical, dental, vision, life and disability plans for eligible employees and their dependents. Additionally, Natera employees and their immediate families receive free testing in addition to fertility care benefits. Other benefits include pregnancy and baby bonding leave, 401k benefits, commuter benefits and much more. We also offer a generous employee referral program!

For more information, visit www.natera.com.

Natera is proud to be an Equal Opportunity Employer. We are committed to ensuring a diverse and inclusive workplace environment, and welcome people of different backgrounds, experiences, abilities and perspectives. Inclusive collaboration benefits our employees, our community and our patients, and is critical to our mission of changing the management of disease worldwide.

All qualified applicants are encouraged to apply, and will be considered without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, age, veteran status, disability or any other legally protected status. We also consider qualified applicants regardless of criminal histories, consistent with applicable laws.

If you are based in California, we encourage you to read this important information for California residents.

Link: https://www.natera.com/notice-of-data-collection-california-residents/

Please be advised that Natera will reach out to candidates with a @natera.com email domain ONLY. Email communications from all other domain names are not from Natera or its employees and are fraudulent. Natera does not request interviews via text messages and does not ask for personal information until a candidate has engaged with the company and has spoken to a recruiter and the hiring team. Natera takes cyber crimes seriously, and will collaborate with law enforcement authorities to prosecute any related cyber crimes.
<div>
For more information: 
<ul><li>BBB announcement on job scams</li><li>FBI Cyber Crime resource page</li></ul></div></div></div>

Associate Scientist, R&D

Mercor

<div>
 
 About The Job
 
 
 
 
 Mercor
 
 connects elite creative and technical talent with leading AI research labs. Headquartered in San Francisco, our investors include
 
 Benchmark
 
 ,
 
 General Catalyst
 
 ,
 
 Peter Thiel
 
 ,
 
 Adam D'Angelo
 
 ,
 
 Larry Summers
 
 , and
 
 Jack Dorsey
 
 .
 
 
 
 Position:
 
 Life Sciences AI Specialist
 
 
 
 Type:
 
 
 Contract
 
 
 
 
 Compensation:
 
 
 $73/hour
 
 
 
 
 Location:
 
 
 Remote
 
 
 
 
 Role Responsibilities
 
 
 
 <ul>
 <li>
 Write and refine prompts to guide model behavior in the life sciences context.
 </li>
 <li>
 Evaluate LLM-generated responses to biology-related queries for scientific accuracy and reasoning quality.
 </li>
 <li>
 Conduct fact-checking using authoritative public sources and domain knowledge.
 </li>
 <li>
 Annotate model responses by identifying strengths, areas of improvement, and factual or conceptual inaccuracies.
 </li>
 <li>
 Assess clarity, structure, and appropriateness of explanations for different audiences.
 </li>
 <li>
 Ensure model responses align with expected conversational behavior and system guidelines.
 
 
 
 </li>
 </ul>
 
 Qualifications
 
 
 
 
 Must-Have
 
 
 
 <ul>
 <li>
 PhD in Biology or a closely related life sciences field
 </li>
 <li>
 Deep expertise in Molecular &amp; Cellular Biology, Organismal Physiology &amp; Development, Microbiology, Immunology &amp; Pathobiology, or Ecology, Evolution &amp; Environmental Biology
 </li>
 <li>
 Significant experience using large language models (LLMs)
 </li>
 <li>
 Excellent writing skills to clearly explain complex life sciences concepts
 </li>
 <li>
 Strong attention to detail
 </li>
 <li>
 Experience reviewing or editing technical or academic writing
 
 
 
 </li>
 </ul>
 
 Preferred
 
 
 
 <ul>
 <li>
 Prior experience with RLHF, model evaluation, or data annotation work
 </li>
 <li>
 Experience teaching, mentoring, or explaining life sciences concepts to non-expert audiences
 </li>
 <li>
 Familiarity with evaluation rubrics, benchmarks, or structured review frameworks
 
 
 
 </li>
 </ul>
 
 Application Process (Takes 20&ndash;30 mins to complete)
 
 
 
 <ul>
 <li>
 Upload resume
 </li>
 <li>
 AI interview based on your resume
 </li>
 <li>
 Submit form
 
 
 
 </li>
 </ul>
 
 Resources &amp; Support
 
 
 
 <ul>
 <li>
 For details about the interview process and platform information, please check: https://talent.docs.mercor.com/welcome/welcome
 </li>
 <li>
 For any help or support, reach out to: support@mercor.com
 
 
 
 </li>
 </ul>
 
 PS: Our team reviews applications daily. Please complete your AI interview and application steps to be considered for this opportunity.
 
</div>

Molecular Biology Researcher

CRISPR Therapeutics

<div>Job Description:
Company Overview
Since its inception over a decade ago, CRISPR Therapeutics has transformed from a research-stage company advancing programs in the field of gene editing, to a company with a diverse portfolio of product candidates across a broad range of disease areas including hemoglobinopathies, oncology, regenerative medicine, cardiovascular and rare diseases. The Nobel Prize-winning CRISPR science has revolutionized biomedical research and represents a powerful, clinically validated approach with the potential to create a new class of potentially transformative medicines. To accelerate and expand its efforts, CRISPR Therapeutics has established strategic partnerships with leading companies including Vertex Pharmaceuticals. CRISPR Therapeutics AG is headquartered in Zug, Switzerland, with its wholly-owned U.S. subsidiary, CRISPR Therapeutics, Inc., and R&amp;D operations based in Boston, Massachusetts and San Francisco, California.
Position Summary
We are seeking a Senior Research Associate to join our next generation sequencing (NGS) wet lab. The successful candidate will be responsible for the execution of various molecular assays and NGS library preparation workflows to support the development of novel genetic therapies for serious diseases. This position requires enthusiasm, attention to detail, collaborative spirit, and a desire to create new medicines for patients. This position reports to the Associate Director, Genomics.
Responsibilities<ul><li>
Perform DNA/RNA extractions from biological samples, including blood/plasma, primary cells, and tissue samples</li><li>
Transform nucleic acid samples into next generation sequencing libraries for a variety of downstream applications using manual or automated methods
</li><li>Perform routine quality control experiments on sequencing libraries (fluorescent quantification, capillary electrophoresis, and qPCR) and prepare samples for sequencing</li><li>
Maintain sequencing instrumentation and laboratory facilities; troubleshoot instrument and sequencing issues</li><li>
Attend project team meetings and communicate effectively across functional teams to ensure timely completion of concurrent projects</li><li>
Track sample data and project timelines through a laboratory information management system (LIMS) and electronic laboratory notebook (ELN)</li></ul>
Minimum Qualifications<ul><li>
BS/MS in biology or related discipline</li><li>
Industry Experience<ul><li>
Senior Research Associate &ndash; 4-7+ years or 2-5+ years with advanced degree</li></ul></li><li>
Proven experience in NGS library preparation including amplicon sequencing, target enrichment, long read technologies, &amp; WGS</li><li>
Hands-on experience with Illumina next generation sequencing (NGS) instruments</li><li>
Proficiency in relevant areas of molecular biology and genetics</li><li>
Experience working collaboratively with wet and dry lab scientists, and understanding large data sets</li><li>
Excellent organizational and communication skills</li><li>
Ability to think strategically, manage time efficiently, and work independently in a results-oriented research team</li></ul>
Preferred Qualifications<ul><li>
Prior research experience in the biotech industry with a focus on next generation sequencing</li><li>
Experience with Hamilton liquid handlers, Illumina BaseSpace, and a laboratory information management system (LIMS)</li><li>
Experience with NGS-based assay development and troubleshooting</li><li>
Experience with long-read sequencing technologies such as Oxford Nanopore or PacBio</li><li>
Experience with gene editing technologies</li></ul>
Competencies<ul><li>
Collaborative &ndash; Openness, One Team</li><li>
Undaunted &ndash; Fearless, Can-do attitude</li><li>
Results Oriented &ndash; Delivering progress toward our mission. Sense of urgency in solving problems.</li><li>
Entrepreneurial Spirit &ndash; Proactive. Ownership mindset.</li></ul>
CRISPR Therapeutics believes in fostering a dynamic workplace that balances remote work flexibility with the benefits of in-person interactions. Our employees work at least three days on-site, creating a collaborative work environment, where we cultivate mentorship opportunities, increase cross-functional communication and offer opportunities for our employees to connect. Certain lab based and manufacturing positions are located fully on-site.
Senior Manager: Base pay range of $98,000 to $108,000+ bonus, equity and benefits
The range provided is CRISPR Therapeutics&rsquo; reasonable estimate of the base compensation for this role. The actual amount will be based on job-related and non-discriminatory factors such as experience, training, skills, and abilities.
CRISPR Therapeutics, Inc. is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law.
To view our Privacy Statement, please click the following link: http://www.crisprtx.com/about-us/privacy-policy</div>

Senior Research Associate, GACT

Bristol Myers Squibb

<div>Working with Us 
Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. 
 
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us . 
 
The Cell Therapy Thematic Research Center is one of BMS's differentiated research platforms delivering innovative therapies to patients. Our mission is to drive leadership in the use of cellular therapies to harness the power of the immune system in treating hematologic malignancies, solid cancers, and autoimmune disease. More specifically, our discovery and translational scientists are focused on developing next-generation, engineered cell-based therapies. The team is committed to discovering and developing transformative therapies that harness the power of the immune system to improve patient outcomes. 
 
Position Summary: 
 
We are seeking a highly skilled, collaborative, and detail-oriented scientist to join our Translational Research team, bringing deep expertise in CAR T cell therapy and a rigorous scientific foundation in immunology, molecular/cell biology, and/or virology. 
 
In this role, you will serve as a Translational Safety Strategy Lead, driving the evaluation of gene-modified CAR T cell product-related genotoxicity in alignment with established study protocols and applicable regulatory guidelines. Your work will span early- and late-stage clinical programs, with particular emphasis on post-marketing settings, ensuring robust and consistent translational safety oversight across a diverse CAR T portfolio. 
 
Position Responsibilities:<ul><li>
Lead end-to-end translational safety strategies, testing, and reporting across multiple assets and platforms, spanning clinical and commercial programs, ensuring critical alignment with research, clinical development, and medical affair objectives.</li><li>
Oversee complex testing operations, including sample testing workflows, case tracking, data flow, and data management operations; lead in-depth complex case investigations across clinical and commercial settings with scientific rigor and operational precision.</li><li>
Drive continuous process improvements, streamlining data reporting flows and optimizing testing workflows, assay services, and data reporting infrastructure; drive cross-functional efficiency through proactive operational dialogue and stakeholder engagement.</li><li>
Provide scientific leadership and interpretation, integrating translational safety data to inform critical clinical and regulatory decision-making; serve as a subject matter expert contributing scientific insights to health authority inquiries and regulatory submissions.</li><li>
Operate effectively in a fast-paced, highly matrixed environment , setting priorities with clarity, confidence, and adaptability , cultivating a collaborative and inclusive team culture, and building and sustaining strategic partnerships both internally and externally.</li></ul>
Basic Qualifications:
<ul><li>Bachelor's Degree<ul><li>
8+ years of academic and / or industry experience</li></ul></li></ul>
Or<ul><li>
Master's Degree<ul><li>
6+ years of academic and / or industry experience</li></ul></li></ul>
Or<ul><li>
Ph.D. or equivalent advanced degree in Life Sciences<ul><li>
4+ of academic and / or industry experience</li></ul></li></ul>
Preferred Qualifications:<ul><li>
Ph.D. with 7+ years of combined experience in clinical trial research and basic sciences, including industry and/or biotech settings, with strong background in cell therapy, immunology, molecular/cell biology, and/or virology.</li><li>
Exceptional scientific communication and writing skills, with demonstrated track record in manuscript writing and proven ability to collaborate effectively across cross-functional teams in a fast-paced, highly matrixed environment while managing completing priorities and tight timelines.</li><li>
Strong working knowledge of regulatory frameworks and requirements, including hands-on experience drafting and reviewing regulatory documents, supporting regulatory inquiries and submissions, and contributing to translational strategy development.</li></ul>
#LI-Onsite 
 
If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.
 
 
Compensation Overview: 
 
Seattle - WA: $152,360 - $184,628 
 
The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee's work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience.
 
 
Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit https://careers.bms.com/life-at-bms/.
 
 
Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:
<ul><li>Health Coverage: Medical, pharmacy, dental, and vision care.</li><li>
Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).
</li><li>Financial Well-being and Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.
</li></ul>Work-life benefits include:
 
 
Paid Time Off
<ul><li>US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)
</li><li>Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays
</li></ul>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.
 
 
All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown. 
 
<ul><li>Eligibility Disclosure: T he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.
</li></ul> 
Uniquely Interesting Work, Life-changing Careers 
With a single vision as inspiring as Transforming patients' lives through science&trade; , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. 
 
On-site Protocol 
 
BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:
 
 
Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.
 
 
Supporting People with Disabilities 
 
BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com . Visit careers.bms.com/ eeo -accessibility to access our complete Equal Employment Opportunity statement.
 
 
Candidate Rights 
 
BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
 
 
If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/
 
 
Data Protection 
 
We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection . 
 
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. 
 
If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at TAEnablement@bms.com . Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.
 
 
R1600332 : Principal Scientist, Translational Research - Translational Safety Strategy</div>

Principal Scientist, Translational Research - Translational Safety Strategy

<div>POSITION SUMMARY:

The Senior Research Associate within the Molecular Biology product development team will join a cross-functional team of scientists who are tasked with developing and advancing Natera's oncology product portfolio. We are looking for a meticulous and dedicated individual with experience in both assay development and high throughput automation that can work effectively in a fast-paced environment to ensure that the highest quality clinical assays are developed and launched for our patients.

The ideal candidate is a driven professional who is eager to learn, maintains broad knowledge of molecular biology principles and possesses strong wet lab skills. This position requires flexibility to work outside standard business hours, including some evenings and weekends, to address urgent issues, support high-priority projects, and maintain uninterrupted lab operations.

PRIMARY RESPONSIBILITIES:
<ul>
<li>Assist in design, developing, and validating automated high-throughput NGS assays that will be run in a commercial CLIA laboratory</li>
<li>Participate in post-launch surveillance by troubleshooting production issues, performing root cause analysis on automation, reagent, peripheral equipment and assay failures</li>
<li>With some supervision, design and execute low to moderate complexity experiments</li>
<li>Coordinate across multiple internal groups (automation engineering, laboratory operations, bioinformatics, statistics, project and product management) and serve as point person to ensure the successful identification and timely execution of projects</li>
<li>Draft documentation and SOPs, train lab operations operators on protocols</li>
</ul>
 QUALIFICATIONS:
<ul>
<li>BA/BS with 4 years experience or MS with 2 years experience in assay development and automation for the genomics</li>
<li>Experience participating in development and validation of automated protocols for CLIA. Individuals with no experience in process development will be considered if they can demonstrate strong analytical skills</li>
</ul>
 KNOWLEDGE, SKILLS, AND ABILITIES:
<ul>
<li>Strong understanding of the chemistry underlying nucleic acid extraction, PCR, NGS library preparation, and hybrid capture technologies</li>
<li>Hands-on experience in NGS-based assays</li>
<li>Experience implementing, optimizing, and troubleshooting high-throughput automated assays utilizing liquid handler robots</li>
<li>Dedicated team player aspiring to develop into a strong individual contributor</li>
<li>Data analysis (JMP or similar) is a strong plus</li>
<li>Experience working in a regulated laboratory environment under CLIA/CAP, NYSDOH, IVD is a plus</li>
<li>Excellent communication, organizational, record-keeping, planning, attention to detail and time management skills</li>
<li>Ability to collaborate cross-functionally with other groups (Lab operations, Engineering, Automation)</li></ul><div> 
OUR OPPORTUNITY

Natera&trade; is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women's health, and organ health. Our aim is to make personalized genetic testing and diagnostics part of the standard of care to protect health and enable earlier and more targeted interventions that lead to longer, healthier lives.

The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory scientists, business professionals, software engineers and many other professionals from world-class institutions, who care deeply for our work and each other. When you join Natera, you'll work hard and grow quickly. Working alongside the elite of the industry, you'll be stretched and challenged, and take pride in being part of a company that is changing the landscape of genetic disease management.

WHAT WE OFFER

Competitive Benefits - Employee benefits include comprehensive medical, dental, vision, life and disability plans for eligible employees and their dependents. Additionally, Natera employees and their immediate families receive free testing in addition to fertility care benefits. Other benefits include pregnancy and baby bonding leave, 401k benefits, commuter benefits and much more. We also offer a generous employee referral program!

For more information, visit www.natera.com.

Natera is proud to be an Equal Opportunity Employer. We are committed to ensuring a diverse and inclusive workplace environment, and welcome people of different backgrounds, experiences, abilities and perspectives. Inclusive collaboration benefits our employees, our community and our patients, and is critical to our mission of changing the management of disease worldwide.

All qualified applicants are encouraged to apply, and will be considered without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, age, veteran status, disability or any other legally protected status. We also consider qualified applicants regardless of criminal histories, consistent with applicable laws.

If you are based in California, we encourage you to read this important information for California residents.

Link: https://www.natera.com/notice-of-data-collection-california-residents/

Please be advised that Natera will reach out to candidates with a @natera.com email domain ONLY. Email communications from all other domain names are not from Natera or its employees and are fraudulent. Natera does not request interviews via text messages and does not ask for personal information until a candidate has engaged with the company and has spoken to a recruiter and the hiring team. Natera takes cyber crimes seriously, and will collaborate with law enforcement authorities to prosecute any related cyber crimes.
<div>
For more information: 
<ul><li>BBB announcement on job scams</li><li>FBI Cyber Crime resource page</li></ul></div></div></div>

Senior Research Associate

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